QA Compliance Officer GMP
Location: BelgiumSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Flandre Orientale Belgium.
- Knowledge of GMP.
- Several years of relevant professional experience in an industrial environment.
- You possess a proven track record of project and change management skills.
- Dutch and English (spoken and written).
- Excellent IT-skills (eg Outlook, Word, Excel, Powerpoint). SAP and Sharepoint are a pre
- Proven experience with Operational Excellence (Lean/sigma) is an asset
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
The Company
A leader in the Pharmaceutical industry with a manufacture for the production of API's and intermediates.Role Description
You are responsible to stay abreast with external GMP and regulatory and customer requirements and you will implement and audit them in daily operations.Responsibilities
You will ensure a qualitative and efficient management of authority inspections and customer audits. Furthermore ensure an adequate CAPA management and business continuity according to regulatory, market and customer standards by managing compliance activities.Requirements
- Master or Engineering degree in Chemistry / Sciences.- Knowledge of GMP.
- Several years of relevant professional experience in an industrial environment.
- You possess a proven track record of project and change management skills.
- Dutch and English (spoken and written).
- Excellent IT-skills (eg Outlook, Word, Excel, Powerpoint). SAP and Sharepoint are a pre
- Proven experience with Operational Excellence (Lean/sigma) is an asset
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
Job Description
SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Flandre Orientale Belgium.
- Knowledge of GMP.
- Several years of relevant professional experience in an industrial environment.
- You possess a proven track record of project and change management skills.
- Dutch and English (spoken and written).
- Excellent IT-skills (eg Outlook, Word, Excel, Powerpoint). SAP and Sharepoint are a pre
- Proven experience with Operational Excellence (Lean/sigma) is an asset
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
The Company
A leader in the Pharmaceutical industry with a manufacture for the production of API's and intermediates.Role Description
You are responsible to stay abreast with external GMP and regulatory and customer requirements and you will implement and audit them in daily operations.Responsibilities
You will ensure a qualitative and efficient management of authority inspections and customer audits. Furthermore ensure an adequate CAPA management and business continuity according to regulatory, market and customer standards by managing compliance activities.Requirements
- Master or Engineering degree in Chemistry / Sciences.- Knowledge of GMP.
- Several years of relevant professional experience in an industrial environment.
- You possess a proven track record of project and change management skills.
- Dutch and English (spoken and written).
- Excellent IT-skills (eg Outlook, Word, Excel, Powerpoint). SAP and Sharepoint are a pre
- Proven experience with Operational Excellence (Lean/sigma) is an asset
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Quality Control / Production Audit
